Cited 0 times in
Current insights in ultra-rare adenylosuccinate synthetase 1 myopathy - meeting report on the First Clinical and Scientific Conference. 3 June 2024, National Centre for Advancing Translational Science, Rockville, Maryland, the United States of America
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 박형준 | - |
dc.date.accessioned | 2025-02-03T09:23:42Z | - |
dc.date.available | 2025-02-03T09:23:42Z | - |
dc.date.issued | 2024-11 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/202427 | - |
dc.description.abstract | The inaugural Clinical and Scientific Conference on Adenylosuccinate Synthetase 1 (ADSS1) myopathy was held on June 3, 2024, at the National Institutes of Health (NIH) National Center for Advancing Translational Sciences (NCATS) in Rockville, Maryland, USA. ADSS1 myopathy is an ultra-rare, inherited neuromuscular disease. Features of geographical patient clusters in South Korea, Japan, India and the United States of America were characterised and discussed. Pre-clinical animal and cell-based models were discussed, providing unique insight into disease pathogenesis. The biochemical pathogenesis was discussed, and potential therapeutic targets identified. Potential clinical and pre-clinical biomarkers were discussed. An ADSS1 myopathy consortium was established and a roadmap for therapeutic development created. | - |
dc.description.statementOfResponsibility | open | - |
dc.language | English | - |
dc.publisher | BioMed Central | - |
dc.relation.isPartOf | ORPHANET JOURNAL OF RARE DISEASES | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.title | Current insights in ultra-rare adenylosuccinate synthetase 1 myopathy - meeting report on the First Clinical and Scientific Conference. 3 June 2024, National Centre for Advancing Translational Science, Rockville, Maryland, the United States of America | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Neurology (신경과학교실) | - |
dc.contributor.googleauthor | Emma Rybalka | - |
dc.contributor.googleauthor | Hyung Jun Park | - |
dc.contributor.googleauthor | Atchayaram Nalini | - |
dc.contributor.googleauthor | Dipti Baskar | - |
dc.contributor.googleauthor | Kiran Polavarapu | - |
dc.contributor.googleauthor | Hacer Durmus | - |
dc.contributor.googleauthor | Yang Xia | - |
dc.contributor.googleauthor | Linlin Wan | - |
dc.contributor.googleauthor | Perry B Shieh | - |
dc.contributor.googleauthor | Behzad Moghadaszadeh | - |
dc.contributor.googleauthor | Alan H Beggs | - |
dc.contributor.googleauthor | David L Mack | - |
dc.contributor.googleauthor | Alec S T Smith | - |
dc.contributor.googleauthor | Wendy Hanna-Rose | - |
dc.contributor.googleauthor | Hyder A Jinnah | - |
dc.contributor.googleauthor | Cara A Timpani | - |
dc.contributor.googleauthor | Min Shen | - |
dc.contributor.googleauthor | Jaymin Upadhyay | - |
dc.contributor.googleauthor | Jeffrey J Brault | - |
dc.contributor.googleauthor | Matthew D Hall | - |
dc.contributor.googleauthor | Naveen Baweja | - |
dc.contributor.googleauthor | Priyanka Kakkar | - |
dc.identifier.doi | 10.1186/s13023-024-03429-x | - |
dc.contributor.localId | A01758 | - |
dc.relation.journalcode | J03433 | - |
dc.identifier.eissn | 1750-1172 | - |
dc.identifier.pmid | 39593137 | - |
dc.subject.keyword | ADSS1 myopathy | - |
dc.subject.keyword | Adenylosuccinate synthetase 1 myopathy | - |
dc.subject.keyword | Biomarkers | - |
dc.subject.keyword | Cardiac muscle | - |
dc.subject.keyword | Clinical presentation | - |
dc.subject.keyword | Consortium | - |
dc.subject.keyword | Guidelines | - |
dc.subject.keyword | Inborn error of metabolism | - |
dc.subject.keyword | Pre-clinical models | - |
dc.subject.keyword | Purine disorder | - |
dc.subject.keyword | Skeletal muscle | - |
dc.subject.keyword | Therapeutics | - |
dc.subject.keyword | Ultra-rare neuromuscular disease | - |
dc.contributor.alternativeName | Park, Hyung Jun | - |
dc.contributor.affiliatedAuthor | 박형준 | - |
dc.citation.volume | 19 | - |
dc.citation.startPage | 438 | - |
dc.identifier.bibliographicCitation | ORPHANET JOURNAL OF RARE DISEASES, Vol.19 : 438, 2024-11 | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.